Controlled Delivery of Theophylline: Chemistry of 7-acyl- and 7,7'-acylditheophylline Derivates
Overview
Pharmacy
Affiliations
7-Acyl- and 7,7'-acylditheophylline derivatives were prepared from the reaction of theophylline with acid chlorides. In addition, a novel synthesis of these compounds was developed, which proceeds through an acylonium ion generated under mild conditions. The physical properties and stability of the derivative of choice, 7,7'-succinylditheophylline, depend on the synthetic procedure employed. This compound is a useful controlled-release prodrug of theophylline.
PURINE FUNCTIONALIZED CONGENERS AS MOLECULAR PROBES FOR ADENOSINE RECEPTORS.
Jacobson K, Daly J Nucleosides Nucleotides. 2025; 10(5):1029-1038.
PMID: 39802924 PMC: 11724714. DOI: 10.1080/07328319108047240.
Adenosine receptor prodrugs: towards kidney-selective dialkylxanthines.
Barone S, Churchill P, Jacobson K J Pharmacol Exp Ther. 1989; 250(1):79-85.
PMID: 2746513 PMC: 3476460.